US20160145445A1 - Method of preparing carbon-coated manganous oxide and carbon-coated manganous oxide prepared using the method - Google Patents
Method of preparing carbon-coated manganous oxide and carbon-coated manganous oxide prepared using the method Download PDFInfo
- Publication number
- US20160145445A1 US20160145445A1 US14/946,800 US201514946800A US2016145445A1 US 20160145445 A1 US20160145445 A1 US 20160145445A1 US 201514946800 A US201514946800 A US 201514946800A US 2016145445 A1 US2016145445 A1 US 2016145445A1
- Authority
- US
- United States
- Prior art keywords
- coated
- polyacrylonitrile
- carbon
- yield
- lpan
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 62
- 229910052799 carbon Inorganic materials 0.000 title claims abstract description 61
- PPNAOCWZXJOHFK-UHFFFAOYSA-N manganese(2+);oxygen(2-) Chemical compound [O-2].[Mn+2] PPNAOCWZXJOHFK-UHFFFAOYSA-N 0.000 title claims abstract description 60
- VASIZKWUTCETSD-UHFFFAOYSA-N manganese(II) oxide Inorganic materials [Mn]=O VASIZKWUTCETSD-UHFFFAOYSA-N 0.000 title claims abstract description 60
- 238000000034 method Methods 0.000 title claims abstract description 31
- 229920002239 polyacrylonitrile Polymers 0.000 claims abstract description 52
- 150000002697 manganese compounds Chemical class 0.000 claims abstract description 34
- 239000000203 mixture Substances 0.000 claims abstract description 28
- 239000002904 solvent Substances 0.000 claims abstract description 22
- 239000002243 precursor Substances 0.000 claims abstract description 18
- 239000007788 liquid Substances 0.000 claims abstract description 15
- 238000002156 mixing Methods 0.000 claims abstract description 13
- 238000001354 calcination Methods 0.000 claims abstract description 10
- 238000003756 stirring Methods 0.000 claims abstract description 9
- 238000001035 drying Methods 0.000 claims abstract description 5
- 238000010438 heat treatment Methods 0.000 claims abstract description 5
- 239000011261 inert gas Substances 0.000 claims abstract description 5
- 239000007787 solid Substances 0.000 claims abstract description 4
- 239000002019 doping agent Substances 0.000 claims description 33
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 claims description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 6
- 239000000178 monomer Substances 0.000 claims description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
- 229920002554 vinyl polymer Polymers 0.000 claims description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 5
- 238000000498 ball milling Methods 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 238000002604 ultrasonography Methods 0.000 claims description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 3
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052796 boron Inorganic materials 0.000 claims description 3
- 229910052804 chromium Inorganic materials 0.000 claims description 3
- 239000011651 chromium Substances 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 229920001577 copolymer Polymers 0.000 claims description 3
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 239000010949 copper Substances 0.000 claims description 3
- 229920001519 homopolymer Polymers 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 150000002696 manganese Chemical class 0.000 claims description 3
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 3
- 229910001509 metal bromide Inorganic materials 0.000 claims description 3
- 229910001512 metal fluoride Inorganic materials 0.000 claims description 3
- 229910044991 metal oxide Inorganic materials 0.000 claims description 3
- 150000004706 metal oxides Chemical class 0.000 claims description 3
- 229910052976 metal sulfide Inorganic materials 0.000 claims description 3
- VLCAYQIMSMPEBW-UHFFFAOYSA-N methyl 3-hydroxy-2-methylidenebutanoate Chemical compound COC(=O)C(=C)C(C)O VLCAYQIMSMPEBW-UHFFFAOYSA-N 0.000 claims description 3
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 150000004767 nitrides Chemical class 0.000 claims description 3
- 150000002902 organometallic compounds Chemical class 0.000 claims description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims description 3
- 239000011574 phosphorus Substances 0.000 claims description 3
- 229910052710 silicon Inorganic materials 0.000 claims description 3
- 239000010703 silicon Substances 0.000 claims description 3
- 229910052709 silver Inorganic materials 0.000 claims description 3
- 239000004332 silver Substances 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 239000011593 sulfur Substances 0.000 claims description 3
- 229910052718 tin Inorganic materials 0.000 claims description 3
- 239000011135 tin Substances 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 239000011248 coating agent Substances 0.000 description 14
- 238000000576 coating method Methods 0.000 description 14
- 230000003373 anti-fouling effect Effects 0.000 description 9
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- 238000002441 X-ray diffraction Methods 0.000 description 6
- 125000000524 functional group Chemical group 0.000 description 5
- 238000000227 grinding Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 230000003197 catalytic effect Effects 0.000 description 4
- 239000000919 ceramic Substances 0.000 description 4
- 238000002411 thermogravimetry Methods 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 239000002156 adsorbate Substances 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 230000002349 favourable effect Effects 0.000 description 3
- 239000012705 liquid precursor Substances 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 2
- 238000003763 carbonization Methods 0.000 description 2
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 2
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 description 2
- 229940112669 cuprous oxide Drugs 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 229920002521 macromolecule Polymers 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000009827 uniform distribution Methods 0.000 description 2
- 239000005749 Copper compound Substances 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 150000001880 copper compounds Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
- C09D7/62—Additives non-macromolecular inorganic modified by treatment with other compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/16—Antifouling paints; Underwater paints
- C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
- C09D5/1612—Non-macromolecular compounds
- C09D5/1618—Non-macromolecular compounds inorganic
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/16—Heavy metals; Compounds thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/18—Processes for applying liquids or other fluent materials performed by dipping
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/007—After-treatment
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/02—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by baking
- B05D3/0254—After-treatment
- B05D3/0272—After-treatment with ovens
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/16—Antifouling paints; Underwater paints
- C09D5/1606—Antifouling paints; Underwater paints characterised by the anti-fouling agent
- C09D5/1612—Non-macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/02—Ingredients treated with inorganic substances
Definitions
- the invention relates to a method of preparing carbon-coated manganous oxide (MnO) as well as carbon-coated manganous oxide prepared using the method.
- Cuprous oxide is a common marine antifouling coating.
- copper compounds are toxic.
- Manganous oxide is cheap and abundant in the nature, so it is a promising substitute for cuprous oxide.
- manganous oxide is relatively unstable, which greatly limits its antifouling potential.
- the prepared carbon-coated manganous oxide is stable at room temperature, and has a practicable release speed and long antifouling life.
- a method of preparing carbon-coated manganous oxide comprising:
- a dopant is added to and uniformly mixed with the cyclized LPAN solution.
- a mass ratio of the dopant to the LPAN solution is between 0.01:1 and 0.5:1.
- the dopant is a metallic dopant or a non-metallic dopant
- the metallic dopant is a pure metal comprising tin, copper, silver, aluminum, chromium, iron, manganese, titanium, nickel, and cobalt, or a metal oxide, metal nitride, metal boride, metal fluoride, metal bromide, metal sulfide, organometallic compound, or a mixture thereof
- the non-metallic dopant is silicon, phosphorus, boron, nitrogen, carbon, sulfur, or a compound thereof, or a mixture thereof.
- the liquid polyacrylonitrile (LPAN) solution employs liquid polyacrylonitrile as a solute and contains no solvent, and the LPAN has a relative molecular weight of between 106 and 100000.
- the PLAN is a homopolymer of acrylonitrile, or a copolymer of acrylonitrile and a vinyl monomer.
- the vinyl monomer is selected from the group of styrene, methyl methacrylate, hydroxyethyl methylacrylate, acrylic acid, itaconic acid.
- the uniform mixing of the mixture and the solvent is achieved by stirring, ultrasound, or ball milling.
- the manganese compound is manganese dioxide (MnO 2 ) or a manganese salt.
- the invention also provides a carbon-coated manganous oxide, which is prepared according to the mentioned-above method.
- the obtained carbon-coated manganous oxide has good compatibility with carbon source and the carbon membrane is porous, so that the release speed of manganous oxide can be effectively controlled, which is favorable for the carbon-coated manganous oxide to be used as an antifouling additive for marine antifouling paints.
- the outer coating of polyacrylonitrile can prevent the oxidation of manganous oxide, and the manganous oxide can be slowly released to the surface of the coating via the porous coating, which increases the contact area of the adsorbate and the catalyst, and improves the catalytic performance.
- the method of the invention involves a simple process and low production costs, and the resulting carbon-coated manganous oxide has high purity, high yield, uniform distribution of particle sizes, and good morphology.
- the LPAN solution contains multiple functional groups, and as a liquid precursor, after being modified using a dopant, the LPAN can uniformly mix with and bind to the dopant.
- FIG. 1A is a SEM pattern of a product prepared in Example 1, where the product is prepared at a calcination temperature of 300° C.;
- FIG. 1B is a SEM pattern of a product prepared in Example 1, where the product is prepared at a calcination temperature of 500° C.;
- FIG. 1C is a SEM pattern of a product prepared in Example 1, where the product is prepared at a calcination temperature of 700° C.;
- FIG. 1D is a SEM pattern of a product prepared in Example 1, where the product is prepared at a calcination temperature of 900° C.;
- FIG. 2A is a SEM pattern of a product prepared in Example 2, where the product is carbon-coated manganous oxide;
- FIG. 2B is a SEM pattern of a product prepared in Example 3, where the product is carbon-coated manganous oxide;
- FIG. 2C is a SEM pattern of a product prepared in Example 4, where the product is carbon-coated manganous oxide;
- FIG. 3 is an XRD pattern of a product prepared in Example 1, where the product is carbon-coated manganous oxide;
- FIG. 4 is an XRD pattern of products having different weight percentages of manganese
- FIG. 5 is a thermogravimetric analysis graph of carbon-coated manganous oxide products having different manganous contents in the air atmosphere.
- FIG. 6 is a thermogravimetric analysis graph of carbon-coated manganous oxide products comprising 50 wt. % and 60 wt. % of MnO, respectively, in the air atmosphere at a constant temperature for 10 hours.
- the carbon-coated manganous oxide resulting from solvent thermal treatment has good compatibility with carbon source and the carbon membrane is porous, so that the release speed of manganous oxide can be effectively controlled, which is favorable for the carbon-coated manganous oxide to be used as an antifouling additive for marine antifouling paints.
- the outer coating of polyacrylonitrile can prevent the oxidation of manganous oxide, and the manganous oxide can be slowly released to the surface of the coating via the porous coating, thereby increasing the contact area of the adsorbate and catalyst, and improving the catalytic performance.
- the invention provides a method of preparing a carbon-coated manganous oxide, the method comprising:
- the liquid LPAN solution is stirred at the temperature of between 100 and 200° C. for between 100 and 200 hrs to yield the cyclized polyacrylonitrile solution.
- the linear LPAN molecule is transformed into a thermostable ladder structure, which can resist the pyrolysis during the high-temperature carbonization, thereby ensuring the high carbon residue rate and stable physicochemical properties.
- a carbon layer having a grapheme-like structure is formed.
- the invention employs the PLAN instead of dilute PLAN as a carbon source and solute, and the liquid polyacrylonitrile has a relative molecular weight of between 106 and 100000, particularly, between 150 and 25000.
- the PLAN contains no solvent.
- the polymer is a long chain macromolecule with high molecular weight and high carbon content, and thus provides a structure base for the carbon coating.
- the LPAN is a homopolymer of acrylonitrile, or a copolymer of acrylonitrile and a vinyl monomer
- the vinyl monomer is selected from the group of styrene, methyl methacrylate, hydroxyethyl methylacrylate, acrylic acid, itaconic acid.
- the invention employs the self-made PLAN as a carbon source, and the former presents a liquid in the temperature of between minus 80° C. and 200° C., with a concentration of 0.8 and 1.2 g/cm 2 .
- the polymer is a long chain macromolecule with high molecular weight and high carbon content, and thus provides a structure base for the carbon coating.
- a dopant is added to and uniformly mixed with the cyclized LPAN solution.
- the LPAN solution contains multiple functional groups, and as a liquid precursor, after being modified using a dopant, the LPAN can uniformly mix with and bind to the dopant.
- a dopant is added to and uniformly mixed with the cyclized LPAN solution, and the mixing is achieved by stirring, ultrasound, or ball milling.
- the mass ratio of the dopant to the LPAN is between 0.01:1 and 0.5:1.
- the cyclized LPAN solution has multiple functional groups, which are adapted to tightly bind to the dopant or carbon material. Part of LPAN functional groups can coordinate with the dopant to achieve compatibility and coating in the molecular level.
- the LPAN and the dopant are fully mixed and contacted.
- the mixing is achieved by ball milling.
- the dopant is a metallic dopant or a non-metallic dopant;
- the metallic dopant is a pure metal comprising tin, copper, silver, aluminum, chromium, iron, manganese, titanium, nickel, and cobalt, or a metal oxide, metal nitride, metal boride, metal fluoride, metal bromide, metal sulfide, organometallic compound, or a mixture thereof;
- the non-metallic dopant is silicon, phosphorus, boron, nitrogen, carbon, sulfur, or a compound thereof, or a mixture thereof.
- the dopant is tin powder.
- the tin-doped PLAN has better stability, and tin powder can further improve the catalytic performance of carbon-coated manganous oxide.
- the heating time is 8 hours, so that the thermally-oxidized polyacrylonitrile has more stable chemical properties.
- the manganese compound is manganese dioxide (MnO 2 ) or a manganese salt.
- the solvent is a hydrophilic solvent or a hydrophobic solvent, and a mass ratio of the mixture of the PLAN and the manganese compound to the solvent is between 0.1:1 and 0.5:1.
- the particle size of the manganese compound is between 8 nm and 100 ⁇ m.
- the manganese compound is sieved using a sieve having a mesh of 200-400 mesh, preferably, 300 mesh.
- the dopant can be further added to a mixture of the thermally-oxidized polyacrylonitrile and the manganese compound, and the mixing is achieved by stirring, ultrasound, or ball milling.
- the further doping can provide better coating effect and compatibility at the molecular level.
- the carbonized precursor coated manganese compound can be ground to be powders.
- the inert gas is nitrogen or argon.
- the invention also provides a carbon-coated manganous oxide prepared according to the above-mentioned method.
- LPAN liquid polyacrylonitrile
- OPAN thermally-oxidized polyacrylonitrile
- the thermally-oxidized polyacrylonitrile was mixed with 10 g of manganese dioxide and 20 mL of a solvent.
- the resulting mixture was ball milled using a planetary type ball mill for 10 hrs (400 rad/min), and the ratio of grinding media to material was 7:1. Thereafter, a product was collected and dried in an oven at 220° C.
- thermally-oxidized precursor low temperature carbonization precursor-coated manganese compound
- the thermally-oxidized precursor was calcined in a ceramic boat in the presence of a nitrogen gas flow of 150 mL/min for 4 hrs at the temperature of between 500 and 900° C., and then was cooled to room temperature, to yield carbon-coated manganous oxide.
- the morphologies of the product at the calcination temperature of 300° C., 500° C., 700° C. and 900° C. are shown in FIGS. 1A, 1B, 1C and 1D , respectively.
- the product comprises 80 wt. % of MnO (the material is manganese dioxide, and the product is manganous oxide).
- the XRD pattern thereof is shown in FIG. 3 .
- LPAN liquid polyacrylonitrile
- OPAN thermally-oxidized polyacrylonitrile
- the thermally-oxidized polyacrylonitrile (OPAN) was mixed with 11.25 g of manganese dioxide and 20 mL of a solvent.
- the resulting mixture was ball milled using a planetary type ball mill for 10 hrs (400 rad/min), and the ratio of grinding media to material was 15:1. Thereafter, a product was collected and dried in an oven at 250° C.
- thermally-oxidized precursor was calcined in a ceramic boat in the presence of a nitrogen gas flow of 150 mL/min for 4 hrs at the temperature of 700° C., and then was cooled to room temperature, to yield a mixture of carbon-coated manganous oxide.
- the product comprises 70 wt. % of MnO.
- the morphology thereof is shown in FIG. 2A .
- the XRD pattern thereof is shown in FIG. 4 .
- thermally-oxidized precursor was calcined in a ceramic boat in the presence of an argon gas flow of 150 mL/min for 4 hrs at the temperature of 700° C., and then was cooled to room temperature, to yield a mixture of carbon-coated manganous oxide.
- the product comprises 60 wt. % of MnO.
- the morphology thereof is shown in FIG. 2B .
- the XRD pattern thereof is shown in FIG. 4 .
- LPAN liquid polyacrylonitrile
- OPAN thermally-oxidized polyacrylonitrile
- the thermally-oxidized polyacrylonitrile (OPAN) was mixed with 6.25 g of manganese dioxide and 20 mL of a solvent.
- the resulting mixture was ball milled using a planetary type ball mill for 10 hrs (400 rad/min), and the ratio of grinding media to material was 7:1. Thereafter, a product was collected and dried in an oven at 220° C.
- thermally-oxidized precursor was calcined in a ceramic boat in the presence of an argon gas flow of 150 mL/min for 4 hrs at the temperature of 700° C., and then was cooled to room temperature, to yield a mixture of carbon-coated manganous oxide.
- the product comprises 50 wt. % of MnO.
- the morphology thereof is shown in FIG. 2C .
- the XRD pattern thereof is shown in FIG. 4 .
- FIG. 5 is a thermogravimetric analysis graph of carbon-coated manganous oxide products having different manganous contents in the air atmosphere.
- FIG. 6 is a thermogravimetric analysis graph of carbon-coated manganous oxide products comprising 50 wt. % and 60 wt. % of MnO, respectively, in the air atmosphere at a constant temperature for 10 hours.
- the obtained carbon-coated manganous oxide has good compatibility with carbon source and the carbon membrane is porous, so that the release speed of manganous oxide can be effectively controlled, which is favorable for the carbon-coated manganous oxide to be used as an antifouling additive for marine antifouling paints.
- the outer coating of polyacrylonitrile can prevent the oxidation of manganous oxide, and the manganous oxide are slowly released to the surface of the coating via the porous coating, which increases the contact area of the adsorbate and catalyst, and improves the catalytic performance.
- the method of the invention involves a simple process and low production costs, and the resulting carbon-coated manganous oxide has high purity, high yield, uniform distribution of particle sizes, and good morphology.
- the LPAN solution contains multiple functional groups, and as a liquid precursor, after being modified using a dopant, the LPAN can uniformly mix with and bind to the dopant.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Catalysts (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
- Paints Or Removers (AREA)
Abstract
Description
- Pursuant to 35 U.S.C. §119 and the Paris Convention Treaty, this application claims the benefit of Chinese Patent Application No. 201410666514.0 filed Nov. 20, 2014, the contents of which are incorporated herein by reference.
- 1. Field of the Invention
- The invention relates to a method of preparing carbon-coated manganous oxide (MnO) as well as carbon-coated manganous oxide prepared using the method.
- 2. Description of the Related Art
- Cuprous oxide is a common marine antifouling coating. However, copper compounds are toxic. Manganous oxide is cheap and abundant in the nature, so it is a promising substitute for cuprous oxide. However, manganous oxide is relatively unstable, which greatly limits its antifouling potential.
- In view of the above-described problems, it is one objective of the invention to provide a method of preparing carbon-coated manganous oxide and carbon-coated manganous oxide prepared by the method. The prepared carbon-coated manganous oxide is stable at room temperature, and has a practicable release speed and long antifouling life.
- To achieve the above objective, in accordance with one embodiment of the invention, there is provided a method of preparing carbon-coated manganous oxide, the method comprising:
-
- (1) preparing a liquid polyacrylonitrile (LPAN) solution as a carbon source, stirring the LPAN solution at between 100 and 200° C. for between 100 and 200 hrs to yield a cyclized polyacrylonitrile solution;
- (2) heating the cyclized LPAN solution at between 200 and 300° C. for between 1 and 10 hrs to yield a thermally-oxidized polyacrylonitrile (OPAN) comprising a ladder structure;
- (3) mixing the thermally-oxidized polyacrylonitrile with a manganese compound with a mass ratio thereof being between 0.1:1 and 0.9:1, to yield a mixture, and adding a solvent to the mixture, uniformly mixing, to yield a polyacrylonitrile coated manganese compound;
- (4) drying the polyacrylonitrile coated manganese compound in an oven at a temperature of between 200 and 250° C. for between 1 and 10 hrs until the solvent is evaporated completely and the polyacrylonitrile coated on the manganese compound is crosslinked to form a solid, to yield a carbonized precursor coated manganese compound; and
- (5) calcining the carbonized precursor coated manganese compound in the presence of an inert gas flow of between 10 and 500 mL/min for between 1 and 10 hrs at a temperature of between 500 and 900° C., to yield a carbon-coated manganous oxide.
- In a class of this embodiment, in 1), a dopant is added to and uniformly mixed with the cyclized LPAN solution.
- In a class of this embodiment, a mass ratio of the dopant to the LPAN solution is between 0.01:1 and 0.5:1.
- In a class of this embodiment, the dopant is a metallic dopant or a non-metallic dopant; the metallic dopant is a pure metal comprising tin, copper, silver, aluminum, chromium, iron, manganese, titanium, nickel, and cobalt, or a metal oxide, metal nitride, metal boride, metal fluoride, metal bromide, metal sulfide, organometallic compound, or a mixture thereof; and the non-metallic dopant is silicon, phosphorus, boron, nitrogen, carbon, sulfur, or a compound thereof, or a mixture thereof.
- In a class of this embodiment, the liquid polyacrylonitrile (LPAN) solution employs liquid polyacrylonitrile as a solute and contains no solvent, and the LPAN has a relative molecular weight of between 106 and 100000.
- In a class of this embodiment, the PLAN is a homopolymer of acrylonitrile, or a copolymer of acrylonitrile and a vinyl monomer.
- In a class of this embodiment, the vinyl monomer is selected from the group of styrene, methyl methacrylate, hydroxyethyl methylacrylate, acrylic acid, itaconic acid.
- In a class of this embodiment, in 3), the uniform mixing of the mixture and the solvent is achieved by stirring, ultrasound, or ball milling.
- In a class of this embodiment, in 3), the manganese compound is manganese dioxide (MnO2) or a manganese salt.
- In another aspect, the invention also provides a carbon-coated manganous oxide, which is prepared according to the mentioned-above method.
- Advantages of the method of preparing carbon-coated manganous oxide are summarized as follows. The obtained carbon-coated manganous oxide has good compatibility with carbon source and the carbon membrane is porous, so that the release speed of manganous oxide can be effectively controlled, which is favorable for the carbon-coated manganous oxide to be used as an antifouling additive for marine antifouling paints. In addition, the outer coating of polyacrylonitrile can prevent the oxidation of manganous oxide, and the manganous oxide can be slowly released to the surface of the coating via the porous coating, which increases the contact area of the adsorbate and the catalyst, and improves the catalytic performance. The method of the invention involves a simple process and low production costs, and the resulting carbon-coated manganous oxide has high purity, high yield, uniform distribution of particle sizes, and good morphology. The LPAN solution contains multiple functional groups, and as a liquid precursor, after being modified using a dopant, the LPAN can uniformly mix with and bind to the dopant.
- The invention is described hereinbelow with reference to the accompanying drawings, in which:
-
FIG. 1A is a SEM pattern of a product prepared in Example 1, where the product is prepared at a calcination temperature of 300° C.; -
FIG. 1B is a SEM pattern of a product prepared in Example 1, where the product is prepared at a calcination temperature of 500° C.; -
FIG. 1C is a SEM pattern of a product prepared in Example 1, where the product is prepared at a calcination temperature of 700° C.; -
FIG. 1D is a SEM pattern of a product prepared in Example 1, where the product is prepared at a calcination temperature of 900° C.; -
FIG. 2A is a SEM pattern of a product prepared in Example 2, where the product is carbon-coated manganous oxide; -
FIG. 2B is a SEM pattern of a product prepared in Example 3, where the product is carbon-coated manganous oxide; -
FIG. 2C is a SEM pattern of a product prepared in Example 4, where the product is carbon-coated manganous oxide; -
FIG. 3 is an XRD pattern of a product prepared in Example 1, where the product is carbon-coated manganous oxide; -
FIG. 4 is an XRD pattern of products having different weight percentages of manganese; -
FIG. 5 is a thermogravimetric analysis graph of carbon-coated manganous oxide products having different manganous contents in the air atmosphere; and -
FIG. 6 is a thermogravimetric analysis graph of carbon-coated manganous oxide products comprising 50 wt. % and 60 wt. % of MnO, respectively, in the air atmosphere at a constant temperature for 10 hours. - For further illustrating the invention, experiments detailing a method of preparing a carbon-coated manganous oxide are described below. It should be noted that the following examples are intended to describe and not to limit the invention.
- The carbon-coated manganous oxide resulting from solvent thermal treatment has good compatibility with carbon source and the carbon membrane is porous, so that the release speed of manganous oxide can be effectively controlled, which is favorable for the carbon-coated manganous oxide to be used as an antifouling additive for marine antifouling paints. In addition, the outer coating of polyacrylonitrile can prevent the oxidation of manganous oxide, and the manganous oxide can be slowly released to the surface of the coating via the porous coating, thereby increasing the contact area of the adsorbate and catalyst, and improving the catalytic performance.
- The invention provides a method of preparing a carbon-coated manganous oxide, the method comprising:
- (1) Preparing a liquid polyacrylonitrile (LPAN) solution as a carbon source, stirring the LPAN solution at between 100 and 200° C. for between 100 and 200 hrs to yield a cyclized polyacrylonitrile solution.
- In (1), the liquid LPAN solution is stirred at the temperature of between 100 and 200° C. for between 100 and 200 hrs to yield the cyclized polyacrylonitrile solution. As a result, the linear LPAN molecule is transformed into a thermostable ladder structure, which can resist the pyrolysis during the high-temperature carbonization, thereby ensuring the high carbon residue rate and stable physicochemical properties. In the end, a carbon layer having a grapheme-like structure is formed.
- The invention employs the PLAN instead of dilute PLAN as a carbon source and solute, and the liquid polyacrylonitrile has a relative molecular weight of between 106 and 100000, particularly, between 150 and 25000. The PLAN contains no solvent. The polymer is a long chain macromolecule with high molecular weight and high carbon content, and thus provides a structure base for the carbon coating.
- Preferably, the LPAN is a homopolymer of acrylonitrile, or a copolymer of acrylonitrile and a vinyl monomer, and the vinyl monomer is selected from the group of styrene, methyl methacrylate, hydroxyethyl methylacrylate, acrylic acid, itaconic acid.
- Preferably, the invention employs the self-made PLAN as a carbon source, and the former presents a liquid in the temperature of between minus 80° C. and 200° C., with a concentration of 0.8 and 1.2 g/cm2. The polymer is a long chain macromolecule with high molecular weight and high carbon content, and thus provides a structure base for the carbon coating.
- Preferably, in 1), a dopant is added to and uniformly mixed with the cyclized LPAN solution. The LPAN solution contains multiple functional groups, and as a liquid precursor, after being modified using a dopant, the LPAN can uniformly mix with and bind to the dopant.
- As an improvement, in 1), a dopant is added to and uniformly mixed with the cyclized LPAN solution, and the mixing is achieved by stirring, ultrasound, or ball milling. The mass ratio of the dopant to the LPAN is between 0.01:1 and 0.5:1. The cyclized LPAN solution has multiple functional groups, which are adapted to tightly bind to the dopant or carbon material. Part of LPAN functional groups can coordinate with the dopant to achieve compatibility and coating in the molecular level. After grinding or stirring, the LPAN and the dopant are fully mixed and contacted. Preferably, the mixing is achieved by ball milling.
- Preferably, the dopant is a metallic dopant or a non-metallic dopant; the metallic dopant is a pure metal comprising tin, copper, silver, aluminum, chromium, iron, manganese, titanium, nickel, and cobalt, or a metal oxide, metal nitride, metal boride, metal fluoride, metal bromide, metal sulfide, organometallic compound, or a mixture thereof; and the non-metallic dopant is silicon, phosphorus, boron, nitrogen, carbon, sulfur, or a compound thereof, or a mixture thereof. Preferably, the dopant is tin powder. The tin-doped PLAN has better stability, and tin powder can further improve the catalytic performance of carbon-coated manganous oxide.
- (2) Heating the cyclized LPAN solution at between 200 and 300° C. for between 1 and 10 hrs to yield a thermally-oxidized polyacrylonitrile (OPAN) comprising a ladder structure.
- Preferably, the heating time is 8 hours, so that the thermally-oxidized polyacrylonitrile has more stable chemical properties.
- (3) Mixing the thermally-oxidized polyacrylonitrile with a manganese compound with a mass ratio thereof being between 0.1:1 and 0.9:1, to yield a mixture, and adding a solvent to the mixture, uniformly mixing, to yield a polyacrylonitrile coated manganese compound.
- Preferably, the manganese compound is manganese dioxide (MnO2) or a manganese salt.
- The solvent is a hydrophilic solvent or a hydrophobic solvent, and a mass ratio of the mixture of the PLAN and the manganese compound to the solvent is between 0.1:1 and 0.5:1.
- The particle size of the manganese compound is between 8 nm and 100 μm. The manganese compound is sieved using a sieve having a mesh of 200-400 mesh, preferably, 300 mesh.
- Preferably, the dopant can be further added to a mixture of the thermally-oxidized polyacrylonitrile and the manganese compound, and the mixing is achieved by stirring, ultrasound, or ball milling. The further doping can provide better coating effect and compatibility at the molecular level.
- (4) Drying the polyacrylonitrile coated manganese compound in an oven at a temperature of between 200 and 250° C. for between 1 and 10 hrs until the solvent is evaporated completely and the polyacrylonitrile coated on the manganese compound is crosslinked to form a solid, to yield a carbonized precursor coated manganese compound. Preferably, the drying time is 3 hours. The carbonized precursor coated manganese compound can be ground to be powders.
- (5) Calcining the carbonized precursor coated manganese compound in the presence of an inert gas flow of between 10 and 500 mL/min for between 1 and 10 hrs at a temperature of between 500 and 900° C., to yield a carbon-coated manganous oxide. Preferably, the calcination temperature is 700° C. and the time lasts 4 hours.
- Preferably, the inert gas is nitrogen or argon.
- The invention also provides a carbon-coated manganous oxide prepared according to the above-mentioned method.
- 4 g of liquid polyacrylonitrile (LPAN) solution (molecular weight 4000) were stirred at 120° C. for 120 hrs, to yield a cyclized polyacrylonitrile solution. The cyclized LPAN solution was heated at 300° C. for 8 hrs to yield a thermally-oxidized polyacrylonitrile (OPAN) comprising a ladder structure. The thermally-oxidized polyacrylonitrile was mixed with 10 g of manganese dioxide and 20 mL of a solvent. The resulting mixture was ball milled using a planetary type ball mill for 10 hrs (400 rad/min), and the ratio of grinding media to material was 7:1. Thereafter, a product was collected and dried in an oven at 220° C. for 3 hrs to yield a thermally-oxidized precursor (low temperature carbonization precursor-coated manganese compound). The thermally-oxidized precursor was calcined in a ceramic boat in the presence of a nitrogen gas flow of 150 mL/min for 4 hrs at the temperature of between 500 and 900° C., and then was cooled to room temperature, to yield carbon-coated manganous oxide. The morphologies of the product at the calcination temperature of 300° C., 500° C., 700° C. and 900° C. are shown in
FIGS. 1A, 1B, 1C and 1D , respectively. The product comprises 80 wt. % of MnO (the material is manganese dioxide, and the product is manganous oxide). The XRD pattern thereof is shown inFIG. 3 . - 6 g of liquid polyacrylonitrile (LPAN) solution (molecular weight 4000) were stirred at 120° C. for 120 hrs, to yield a cyclized solution. The cyclized solution was heated at 200° C. for 8 hrs to yield a thermally-oxidized polyacrylonitrile (OPAN) comprising a ladder structure. The thermally-oxidized polyacrylonitrile (OPAN) was mixed with 11.25 g of manganese dioxide and 20 mL of a solvent. The resulting mixture was ball milled using a planetary type ball mill for 10 hrs (400 rad/min), and the ratio of grinding media to material was 15:1. Thereafter, a product was collected and dried in an oven at 250° C. for 3 hrs to yield a thermally-oxidized precursor. The thermally-oxidized precursor was calcined in a ceramic boat in the presence of a nitrogen gas flow of 150 mL/min for 4 hrs at the temperature of 700° C., and then was cooled to room temperature, to yield a mixture of carbon-coated manganous oxide. The product comprises 70 wt. % of MnO. The morphology thereof is shown in
FIG. 2A . The XRD pattern thereof is shown inFIG. 4 . - 8 g of liquid polyacrylonitrile (LPAN) solution (molecular weight 4000) were stirred at 120° C. for 120 hrs to yield a cyclized solution. The cyclized solution was heated at 250° C. for 8 hrs to yield a thermally-oxidized polyacrylonitrile (OPAN) comprising a ladder structure. The thermally-oxidized polyacrylonitrile (OPAN) was mixed with 7.5 g of manganese dioxide and 20 mL of a solvent. The resulting mixture was ball milled using a planetary type ball mill for 10 hrs (400 rad/min), and the ratio of grinding media to material was 7:1. Thereafter, a product was collected and dried in an oven at 280° C. for 3 hrs, to yield a thermally-oxidized precursor. The thermally-oxidized precursor was calcined in a ceramic boat in the presence of an argon gas flow of 150 mL/min for 4 hrs at the temperature of 700° C., and then was cooled to room temperature, to yield a mixture of carbon-coated manganous oxide. The product comprises 60 wt. % of MnO. The morphology thereof is shown in
FIG. 2B . The XRD pattern thereof is shown inFIG. 4 . - 10 g of liquid polyacrylonitrile (LPAN) solution (molecular weight 4000) were stirred at 120° C. for 120 hrs to yield a cyclized solution. The cyclized solution was heated at between 200 and 300° C. for 8 hrs to yield a thermally-oxidized polyacrylonitrile (OPAN) comprising a ladder structure. The thermally-oxidized polyacrylonitrile (OPAN) was mixed with 6.25 g of manganese dioxide and 20 mL of a solvent. The resulting mixture was ball milled using a planetary type ball mill for 10 hrs (400 rad/min), and the ratio of grinding media to material was 7:1. Thereafter, a product was collected and dried in an oven at 220° C. for 3 hrs, to yield a thermally-oxidized precursor. The thermally-oxidized precursor was calcined in a ceramic boat in the presence of an argon gas flow of 150 mL/min for 4 hrs at the temperature of 700° C., and then was cooled to room temperature, to yield a mixture of carbon-coated manganous oxide. The product comprises 50 wt. % of MnO. The morphology thereof is shown in
FIG. 2C . The XRD pattern thereof is shown inFIG. 4 . -
FIG. 5 is a thermogravimetric analysis graph of carbon-coated manganous oxide products having different manganous contents in the air atmosphere. -
FIG. 6 is a thermogravimetric analysis graph of carbon-coated manganous oxide products comprising 50 wt. % and 60 wt. % of MnO, respectively, in the air atmosphere at a constant temperature for 10 hours. - The obtained carbon-coated manganous oxide has good compatibility with carbon source and the carbon membrane is porous, so that the release speed of manganous oxide can be effectively controlled, which is favorable for the carbon-coated manganous oxide to be used as an antifouling additive for marine antifouling paints. In addition, the outer coating of polyacrylonitrile can prevent the oxidation of manganous oxide, and the manganous oxide are slowly released to the surface of the coating via the porous coating, which increases the contact area of the adsorbate and catalyst, and improves the catalytic performance.
- The method of the invention involves a simple process and low production costs, and the resulting carbon-coated manganous oxide has high purity, high yield, uniform distribution of particle sizes, and good morphology. The LPAN solution contains multiple functional groups, and as a liquid precursor, after being modified using a dopant, the LPAN can uniformly mix with and bind to the dopant.
- While particular embodiments of the invention have been shown and described, it will be obvious to those skilled in the art that changes and modifications may be made without departing from the invention in its broader aspects, and therefore, the aim in the appended claims is to cover all such changes and modifications as fall within the true spirit and scope of the invention.
Claims (10)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201410666514 | 2014-11-20 | ||
CN201410666514.0A CN104485456B (en) | 2014-11-20 | 2014-11-20 | The preparation method and carbon coating manganous oxide of a kind of carbon coating manganous oxide |
CN201410666514.0 | 2014-11-20 |
Publications (2)
Publication Number | Publication Date |
---|---|
US20160145445A1 true US20160145445A1 (en) | 2016-05-26 |
US9458330B2 US9458330B2 (en) | 2016-10-04 |
Family
ID=52759979
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US14/946,800 Active US9458330B2 (en) | 2014-11-20 | 2015-11-20 | Method of preparing carbon-coated manganous oxide and carbon-coated manganous oxide prepared using the method |
Country Status (2)
Country | Link |
---|---|
US (1) | US9458330B2 (en) |
CN (1) | CN104485456B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114229805A (en) * | 2021-11-03 | 2022-03-25 | 深圳市本征方程石墨烯技术股份有限公司 | Preparation method and application of nitrogen-doped porous carbon-coated cobalt diselenide composite material |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104979545B (en) * | 2015-06-10 | 2017-08-04 | 苏州冷石纳米材料科技有限公司 | Flower-shaped manganous oxide micro-sphere material and its preparation method and application |
CN105633373B (en) * | 2015-11-06 | 2018-06-22 | 北京化工大学 | A kind of porous manganese monoxide composite material of carbon coating and its preparation method and application |
CN105895950A (en) * | 2016-01-22 | 2016-08-24 | 西北工业大学 | Total manganese lithium-ion battery and preparation method thereof |
CN106450180B (en) * | 2016-09-19 | 2019-02-15 | 广东工业大学 | A kind of lithium ion battery electrode material and preparation method thereof |
CN106981643B (en) * | 2017-05-23 | 2019-07-16 | 山东大学 | A kind of method that biogel carbonization prepares the double-deck carbon coating manganous oxide electrode material |
CN110311099A (en) * | 2018-03-25 | 2019-10-08 | 北京金羽新能科技有限公司 | A kind of carbon coating oxide electrode material and preparation method thereof |
CN110148716B (en) * | 2019-04-24 | 2021-02-05 | 浙江浙能中科储能科技有限公司 | Structure and preparation method of multi-sphere stacked carbon-coated manganese dioxide composite material |
CN113104895A (en) * | 2020-01-13 | 2021-07-13 | 广州汽车集团股份有限公司 | Preparation method of manganous oxide/carbon composite material, negative electrode and lithium ion battery |
CN111916742B (en) * | 2020-07-09 | 2021-09-24 | 江苏理工学院 | Tin-carbon co-doped lithium titanate material and preparation method and application thereof |
CN114220956B (en) * | 2021-12-06 | 2023-03-28 | 厦门理工学院 | Si @ MnO @ C composite material and preparation method thereof, negative electrode material and battery |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100433822B1 (en) * | 2002-01-17 | 2004-06-04 | 한국과학기술연구원 | Metal-coated carbon, preparation method thereof, and composite electrode and lithium secondary batteries comprising the same |
CN103606654B (en) * | 2012-12-21 | 2016-01-06 | 燕山大学 | The preparation method of the coated manganese oxide composite material of a kind of carbon |
CN104031414B (en) * | 2014-06-05 | 2016-02-10 | 深圳市本征方程石墨烯技术股份有限公司 | The preparation method of the coated Red copper oxide of a kind of carbon and the coated Red copper oxide of carbon |
-
2014
- 2014-11-20 CN CN201410666514.0A patent/CN104485456B/en active Active
-
2015
- 2015-11-20 US US14/946,800 patent/US9458330B2/en active Active
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114229805A (en) * | 2021-11-03 | 2022-03-25 | 深圳市本征方程石墨烯技术股份有限公司 | Preparation method and application of nitrogen-doped porous carbon-coated cobalt diselenide composite material |
Also Published As
Publication number | Publication date |
---|---|
CN104485456B (en) | 2017-10-13 |
CN104485456A (en) | 2015-04-01 |
US9458330B2 (en) | 2016-10-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US9458330B2 (en) | Method of preparing carbon-coated manganous oxide and carbon-coated manganous oxide prepared using the method | |
US10163538B2 (en) | Method of preparing graphene-coated alumina and graphene-coated alumina prepared using the method | |
US9761346B2 (en) | Method of preparing copper-based composite conductive powder | |
CN108483444B (en) | Preparation method of alpha-FeOOH nanorod-loaded porous biochar composite material | |
KR100956505B1 (en) | Method of fabricating carbon particle/copper composites | |
US8945501B2 (en) | Method for preparing carbon nanotube or carbon microtube | |
US9630852B2 (en) | Graphene material and method of preparing the same | |
Hwang et al. | Micro‐Blooming: Hierarchically Porous Nitrogen‐Doped Carbon Flowers Derived from Metal‐Organic Mesocrystals | |
CA2840747A1 (en) | Hybrid materials and nanocomposite materials, methods of making same, and uses thereof | |
KR101356990B1 (en) | Iron oxalate hydrate particles with controlled shapes and manufacturing method thereof, iron oxide/carbon composites manufactured by using the iron oxalate hydrate particles and manufacturing method thereof | |
CN108609602B (en) | Nitrogen-doped microporous carbon material based on energetic polyion liquid and preparation method thereof | |
TW201238131A (en) | Electrode materials and process for producing them | |
JP2006062954A (en) | Method of manufacturing activated carbon | |
CN110302753B (en) | Preparation method of magnesium oxide-carbon composite microspheres | |
CN113617355B (en) | Functional mesoporous material embedded with nano particles and in-situ embedding assembly method and application thereof | |
US9399243B1 (en) | Method of preparing carbon-coated cuprous oxide | |
JP2013535395A (en) | Silicon carbide and method for producing the same | |
CN109382084B (en) | Mesoporous carbon material and preparation method and application thereof | |
JP6993640B2 (en) | Nitrogen-containing polycyclic compound | |
KR101615604B1 (en) | Method for preparing catalyst composite including intermetallic nano particle | |
TW201425215A (en) | Method of modifying carbon-based electrode material and carbon-based electrode material formed thereby | |
Teh et al. | ZnCl2/NaCl-catalysed hydrothermal carbonization of glucose and oil palm shell fiber | |
US20220194793A1 (en) | Ordered cross-stacked metal oxide nanowire array material and preparation method thereof | |
US8846135B2 (en) | Process for the preparation of conductive carbon layers on powdered supports | |
CN103740210A (en) | Microporous type nano coating |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: LIU, JIANHONG, CHINA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:LIU, JIANHONG;ZHANG, QIANLING;HE, CHUANXIN;AND OTHERS;REEL/FRAME:037095/0257 Effective date: 20151119 |
|
AS | Assignment |
Owner name: SHENZHEN EIGEN-EQUATION GRAPHENE TECHNOLOGY CO., L Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:LIU, JIANHONG;REEL/FRAME:039590/0823 Effective date: 20160712 |
|
STCF | Information on status: patent grant |
Free format text: PATENTED CASE |
|
MAFP | Maintenance fee payment |
Free format text: PAYMENT OF MAINTENANCE FEE, 4TH YR, SMALL ENTITY (ORIGINAL EVENT CODE: M2551); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY Year of fee payment: 4 |
|
MAFP | Maintenance fee payment |
Free format text: PAYMENT OF MAINTENANCE FEE, 8TH YR, SMALL ENTITY (ORIGINAL EVENT CODE: M2552); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY Year of fee payment: 8 |